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Severe postnatal cytomegalovirus infection with multisystem involvement in an extremely low birth weight infant.严重的产后巨细胞病毒感染伴多系统受累的极低出生体重儿。
J Perinatol. 2012 Jan;32(1):72-4. doi: 10.1038/jp.2011.58.
2
Transmission of cytomegalovirus via breast milk in extremely premature infants.经母乳传播巨细胞病毒在极早产儿中的情况。
J Perinatol. 2011 Jun;31(6):440-5. doi: 10.1038/jp.2010.150. Epub 2010 Dec 16.
3
Is a 6-week course of ganciclovir therapy effective for chorioretinitis in infants with congenital cytomegalovirus infection?更昔洛韦 6 周疗程治疗先天性巨细胞病毒感染婴儿性视网膜炎是否有效?
J Pediatr. 2010 Aug;157(2):331-3. doi: 10.1016/j.jpeds.2010.02.020. Epub 2010 Apr 18.
4
Pp65 antigenemia, plasma real-time PCR and DBS test in symptomatic and asymptomatic cytomegalovirus congenitally infected newborns.Pp65 抗原血症、血浆实时 PCR 和 DBS 检测在有症状和无症状先天性巨细胞病毒感染新生儿中的应用。
BMC Infect Dis. 2010 Feb 11;10:24. doi: 10.1186/1471-2334-10-24.
5
Postnatal cytomegalovirus: innocent bystander or hidden problem?产后巨细胞病毒:无辜旁观者还是隐藏问题?
Arch Dis Child Fetal Neonatal Ed. 2009 Jan;94(1):F58-64. doi: 10.1136/adc.2007.131623. Epub 2008 Oct 6.
6
Pharmacokinetic and pharmacodynamic assessment of oral valganciclovir in the treatment of symptomatic congenital cytomegalovirus disease.口服缬更昔洛韦治疗有症状的先天性巨细胞病毒疾病的药代动力学和药效学评估。
J Infect Dis. 2008 Mar 15;197(6):836-45. doi: 10.1086/528376.
7
Oral valganciclovir for symptomatic congenital cytomegalovirus infection in an extremely low birth weight infant.口服缬更昔洛韦用于治疗极低出生体重儿的有症状先天性巨细胞病毒感染。
J Perinatol. 2008 Jan;28(1):74-6. doi: 10.1038/sj.jp.7211854.
8
Severe postnatal cytomegalovirus infection in a very premature infant.一名极早产儿发生严重的产后巨细胞病毒感染。
Neonatology. 2007;92(4):236-9. doi: 10.1159/000103982. Epub 2007 Jun 15.
9
Effect of ganciclovir therapy on hearing in symptomatic congenital cytomegalovirus disease involving the central nervous system: a randomized, controlled trial.更昔洛韦治疗对累及中枢神经系统的有症状先天性巨细胞病毒病听力的影响:一项随机对照试验。
J Pediatr. 2003 Jul;143(1):16-25. doi: 10.1016/s0022-3476(03)00192-6.
10
Prevention of transfusion-acquired cytomegalovirus infection in infants by blood filtration to remove leucocytes. Neonatal Cytomegalovirus Infection Study Group.通过血液过滤去除白细胞预防婴儿输血获得性巨细胞病毒感染。新生儿巨细胞病毒感染研究组
Lancet. 1989 Jun 3;1(8649):1228-31. doi: 10.1016/s0140-6736(89)92330-1.

一例先前因先天性感染接受治疗的早产儿发生严重迟发性多系统巨细胞病毒感染。

Severe late-onset multisystem cytomegalovirus infection in a premature neonate previously treated for congenital infection.

机构信息

Division of Infectious Disease, Department of Pediatrics, McMaster University, rm 3A-30 1280 Main St, West, Hamilton, ON L8S 4 K1, Canada.

出版信息

BMC Pediatr. 2013 Sep 11;13:142. doi: 10.1186/1471-2431-13-142.

DOI:10.1186/1471-2431-13-142
PMID:24024982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3847698/
Abstract

BACKGROUND

Cytomegalovirus is the most common pathogen causing congenital infection and can result in significant neurodevelopmental adverse outcomes. For this reason, it is the standard of care in many regions to treat congenital cytomegalovirus infection involving the brain with six weeks of ganciclovir. There have been no reports in the published literature of significant cytomegalovirus neonatal infection in infants previously treated for congenital infection.

CASE PRESENTATION

A preterm male infant with congenital symptomatic cytomegalovirus infection was initially treated with over 8 weeks of ganciclovir between the ages of 3 and 14 weeks. At four months chronologic age, just prior to planned discharge, he developed an episode of life-threatening multisystem cytomegalovirus disease notable for severe pneumonitis, encephalitis, hepatitis, and disseminated intravascular coagulation. This disease resolved after re-treatment with a prolonged course of intravenous ganciclovir and oral valganciclovir.

CONCLUSIONS

Clinicians should be aware of the possibility of recurrence of congenital cytomegalovirus infection, especially in preterm infants. Serial plasma cytomegalovirus viral load monitoring may have a role in the management of premature infants treated with ganciclovir; had the diagnosis of recrudescent cytomegalovirus infection been considered sooner, specific therapy might have been more quickly initiated and perhaps further morbidity would have been prevented.

摘要

背景

巨细胞病毒是导致先天性感染的最常见病原体,可导致严重的神经发育不良后果。出于这个原因,在许多地区,用更昔洛韦治疗涉及大脑的先天性巨细胞病毒感染是标准的治疗方法,疗程为六周。在已发表的文献中,没有报道过先前接受先天性感染治疗的新生儿有严重巨细胞病毒感染的病例。

病例介绍

一名患有先天性症状性巨细胞病毒感染的早产儿,在 3 至 14 周龄时最初接受了超过 8 周的更昔洛韦治疗。在 4 个月的月龄时,也就是计划出院前,他出现了危及生命的多系统巨细胞病毒病发作,表现为严重的肺炎、脑炎、肝炎和弥漫性血管内凝血。在重新接受静脉用更昔洛韦和口服缬更昔洛韦的长期治疗后,这种疾病得到了缓解。

结论

临床医生应意识到先天性巨细胞病毒感染复发的可能性,尤其是在早产儿中。对接受更昔洛韦治疗的早产儿进行连续的血浆巨细胞病毒病毒载量监测可能对管理有一定作用;如果更早地考虑到复发性巨细胞病毒感染的诊断,可能会更快地开始特定治疗,或许可以预防进一步的发病。